# FDA recall D-300-2013

> **OPMX, LLC** · Class II · drug recall initiated 2013-04-12.

## Product

Pentrexcilina Jarabe NF (dextromethorphan HBr and guaifenesin) liquid, 118 mL/ 4 fl oz bottle, Distributed by Laboratorios Nordimex Co., San Diego, CA  92154, UPC 0 91965 02001 1.

## Reason for recall

Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading because they may be confused with Pentrexyl, a prescription antibiotic used to treat respiratory illnesses in Mexico.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-300-2013
- **Recalling firm:** OPMX, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-04-12
- **Report date:** 2013-05-01
- **Termination date:** 2013-08-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-300-2013

## Citation

> AI Analytics. FDA recall D-300-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-300-2013. Source: US FDA. Licensed CC0.

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